Trials / Completed
CompletedNCT02748876
Effect of His-Ventricular (HV) Interval Optimisation in Cardiac Resynchronisation Therapy
A Randomised Cross-over Pilot Study of the Effect of His-Ventricular (HV) Interval Optimisation in Cardiac Resynchronisation Therapy
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 14 (actual)
- Sponsor
- Hull University Teaching Hospitals NHS Trust · Other Government
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Cardiac resynchronisation therapy (CRT) is a specialised type of pacemaker used in patients with severe heart failure to improve symptoms and survival. Approximately one third of patients treated with CRT do not notice significant improvement in their symptoms and this may be due to inadequate co-ordination between the upper and lower chambers of the heart (atrioventricular dyssynchrony). The investigators propose a new method to achieve atrioventricular synchrony in CRT based on measurements of electrical conduction from within the heart. Patients referred for CRT implantation at Castle Hill Hospital are eligible to participate. During CRT implantation, additional measurements, will be recorded from within the heart. After implantation, device settings will be adjusted to either standard or electrophysiologically-optimised settings with cross-over at 4 months. The investigators hypothesis is that patients with optimised settings will derive additional benefit compared to patients with standard pacemaker-determined settings.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | His-Ventricular (HV) optimisation | Optimisation of atrioventricular pacing interval |
Timeline
- Start date
- 2016-09-29
- Primary completion
- 2017-04-28
- Completion
- 2018-03-15
- First posted
- 2016-04-22
- Last updated
- 2019-07-17
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT02748876. Inclusion in this directory is not an endorsement.